The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
X‐CHROMOSOME INACTIVATION AND DEVELOPMENTAL PATTERNS IN MAMMALS
Abstract
Summary: 1. The review considers information from mammalian embryology relevant to X‐chromosome inactivation, and from X‐inactivation relevant to mammalian embryology. 2. Properties of the inactive‐X, by which it may be recognized are: sex chromatin, heteropycnosis, late replication and the absence of gene product. Each of these has advantages and disadvantages in particular circumstances. In some species the X carries constitutive heterochromatin, which must be distinguished from the facultative region. 3. The time of X‐chromosome inactivation can be estimated from the time of appearance of sex chromatin or late replication, or inferred from the appearance of heterozygotes for X‐linked genes or of experimental chimaeras. The estimated time varies with species, and in the mouse and rabbit is near the time of increase in RNA synthesis. 4. Whereas in eutherian mammals either the maternally or the paternally derived X may be inactivated in different cell lines, in marsupials the paternal X is always the inactive one. 5. During development various factors act to distort the patterns produced by random X‐inactivation. These factors include cell selection, transfer of gene product, and migration and mingling of cells. 6. There is no clear evidence that X‐chromosome inactivation is not complete. 7. In female germ cells both X‐chromosomes appear to be active. In male ones both X and Y appear inactive during most of spermatogenesis, although probably in early stages all X chromosomes present are active. 8. The active and inactive X‐chromosomes may be differentiated by presence or absence of some non‐histone protein or other polyanionic substance. 9. If the genes concerned in synthesis or attachment of this substance are on the X‐chromosome then the differentiation will be self‐maintaining. 10. The initiation of the differentiation requires either the attachment of different X‐chromosomes to different sites, or some interaction of X‐linked and autosomal genes, concerned in inducing or repressing activity. Some possible models are discussed.
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Citations
Cites
Gene Action in the X-chromosome of the Mouse (Mus musculus L.)
LYON, M. F. (1961) · Nature · doi:10.1038/190372a0 · Cited by 3,978
Self-citation
Cited by
Brown, C. J., Ballabio, A., Rupert, J. L., Lafreniere, R. G., Grompe, M., Tonlorenzi, R., & Willard, H. F. (1991) · Nature · doi:10.1038/349038a0 · Cited by 1,533
Neuronal migration, with special reference to developing human brain: a review
Sidman, R. L., & Rakic, P. (1973) · Brain Research · doi:10.1016/0006-8993(73)90617-3 · Cited by 1,255
Xist-deficient mice are defective in dosage compensation but not spermatogenesis.
Marahrens, Y., Panning, B., Dausman, J., Strauss, W., & Jaenisch, R. (1997) · Genes & Development · doi:10.1101/gad.11.2.156 · Cited by 734
Reactivation of an Inactive Human X Chromosome: Evidence for X Inactivation by DNA Methylation
Mohandas, T., Sparkes, R. S., & Shapiro, L. J. (1981) · Science · doi:10.1126/science.6164095 · Cited by 709
Identification of female carriers of adrenoleukodystrophy
Moser, H. W., Moser, A. E., Trojak, J. E., & Supplee, S. W. (1983) · The Journal of Pediatrics · doi:10.1016/s0022-3476(83)80775-6 · Cited by 99
Metadata
- Authors
- LYON, M. F.
- Venue
- Biological Reviews
- Publisher
- Wiley
- Published
- 1972-01
- Volume
- 47
- Issue
- 1
- Pages
- 1-35
- ISSN
- 0006-3231 (ISSN-L)
- 1464-7931
- 1469-185X
- OpenAlex
- W2007671088
- Cited by
- 654
- References
- 1
- FWCI
- 1.00
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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